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1.
IntroductionIndium-tin-oxide(ITO) has been widely used asthe anode material in organic light-emitting devices(OLEDs) because of its high transmittance in the visi-ble region and low electrical resistivity. In the pastyears, many investigations focused on …  相似文献   
2.
The X-ray crystal structures of a series of lithium quinolates – lithium 8-hydroxyquinolinate (Liq), lithium 2-methyl-8-hydroxyquinolinate (MeLiq), and 2-phenyl-8-hydroxquinolinate (PhLiq), are compared. The substitution at the 2-position of the 8-hydroxyquinoline ligand has significant impact on the aggregation of the lithium complex in the crystalline state. Liq and MeLiq molecules crystallize as hexamers, whereas PhLiq crystallizes as a tetramer. The possible influence of crystal-packing forces on the preferred cluster structure was probed using density functional theory calculations on a systematically varied set of Liq, MeLiq, and PhLiq clusters. For Liq and MeLiq, the observed structures match the most stable computed structures. In the PhLiq case, the observed tetrameric structure is computed to be less stable (+1.2 kcal/mol/monomer) than the lowest energy structure, a hexamer. In this case, solid-state effects probably outweigh small differences in cluster stability.  相似文献   
3.
The improvement of optical and optoelectronic properties of the individual poly [2-methoxy-5- (2-ethylhexyloxy)-1,4-phenylenevinylene] (MEH-PPV), poly[2-methoxy-5-(3,7-dimethyl-octyloxy)-1,4-phenylenevinylene]–End capped with Dimethyl phenyl (OC1C10–PPV–DMP), and poly (9,9′-di- n -octylfluorenyl-2,7-diyl) (F8) was revealed by blending them in ternary hybrid with optimal ratio (F8/2 wt.% MEH-PPV/2 wt.% OC1C10–PPV–DMP). All individual and optimal ternary solutions were prepared via the solution-blending method followed by depositing them onto glass and ITO substrates using spin-coating technique. The semi-crystalline phase of the ternary hybrid and the strong mixing between the conjugated polymers were evidenced by observing the X-ray diffraction patterns that related to F8 into the hybrid diffractogram. The optical and optoelectronic properties of all prepared thin films were investigated in terms of absorption and emission spectra, Commission International d′Eclairage (CIE) coordinates, and current–voltage (I-V) characterizations. Emission peaks at the entire range of visible spectrum can be revealed from the ternary hybrid of the three individual conjugated polymers, producing white emission as evidenced from the emission spectrum and CIE coordinates of the hybrid. Among all fabricated organic light-emitting diodes (OLEDs) devices, the ternary hybrid-based-OLED revealed the best performance in terms of current and turn-on voltage.  相似文献   
4.
合成并表征了高氯酸稀土与二苯基亚砜、苯甲酸的四种四元配合物。经元素分析、稀土络合滴定、摩尔电导率及差热-热重分析,表明四元配合物组成为[REL5L′(ClO4)] (ClO4) (RE= La,Pr,Nd,Eu;L=C6H5SOC6H5,L′=C6H5COO-)。在红外光谱中,第一配体二苯基亚砜的νS O的特征吸收峰出现在1 037cm-1处,而各稀土配合物的νS O向低波数移动到984 ~989 cm-1,红移50 cm-1左右,表明稀土离子与亚砜基团的氧原子之间发生配位作用。第二配体苯甲酸钠的反对称伸缩振动吸收峰νas(COO -)出现在1 550 cm-1,对称伸缩振动吸收峰νs(COO -)出现在1 416 cm-1处,羧基伸缩振动吸收频率差Δn[νas(COO -)-νs(COO -)]值为134cm-1;在所有配合物的红外光谱图中νas(COO -)向高波数方向发生了位移,而νs(COO -)向低波数方向发生了位移,并且Δn值均大于钠盐的Δn值,由此可以认为配合物中羧基是通过单齿方式与稀土离子配位。测定了配合物在丙酮溶液中的摩尔电导率,根据配合物在常见有机溶剂中的摩尔电导率与正负离子的关系结合配合物的红外光谱中高氯酸根离子的四条特征吸收带,表明配合物为1:1型电解质,两个ClO4-无机抗衡阴离子,其中一个在外界,一个进入内界与稀土离子配位。配合物的荧光发射光谱表明,四元配合物的荧光强度比二苯基亚砜高氯酸稀土二元配合物的荧光强度提高469%。磷光光谱表明苯甲酸三重态能级的下限和二苯亚砜三重态能级的上限重叠,导致三重态能级范围扩大,由此可见第二配体的加入提高了配体的三重态能级与Eu3 离子5D0能级的匹配程度。同时在配合物的荧光发射光谱中还可以看到铕离子的电偶极跃迁强度大于磁偶极跃迁,表明稀土离子不处于晶体场的对称中心。在四元配合物中,由于第二配体的加入,往往会降低配合物的对称性,从而增强稀土离子的荧光强度。本文合成的稀土配合物具有良好的荧光性能,而且在室温下稳定,溶解性好,分解温度较高。  相似文献   
5.
近年来,作为第三代有机发光二极管(organic light-emitting diodes, OLED)发光材料的热活化延迟荧光(thermally activated delayed fluorescence, TADF)材料受到了学术界和产业界的广泛关注. TADF分子由于其单线态与三线态之间的能级差较小,三线态激子可以被环境热活化而通过反系间窜越上转换至单线态,理论上可实现100%的激子利用率,从而使得OLED器件外量子效率显著提高.TADF材料被认为是突破高效稳定有机电致蓝光发射瓶颈的潜在解决方案.一般, TADF分子为含有电子给体(donor, D)和电子受体(acceptor, A)的纯有机推拉电子体系.通过改变给体单元和受体单元的结构、数量和取代基及其位置可以有效调节TADF分子的单线态-三线态能级差、前线轨道分布、聚集态结构、电致发光颜色及其性能.同时取代基在调控给、受体单元的推拉电子能力及TADF材料的分子构型、聚集态结构和稳定性等物化特性方面扮演着非常重要的角色.本综述分别对D-A型和多重共振型TADF蓝光分子的取代基效应进行了综述,以期为高效稳定的蓝光TADF分...  相似文献   
6.
《中国化学》2018,36(3):241-246
A new multi‐functional penta‐carbazole/benzophenone hybrid compound 5CzBP was designed and synthesized through a simple one‐step catalyst‐free C—N coupling reaction by using 2,3,4,5,6‐pentafluorobenzophenone and carbazole as starting materials. 5CzBP is very soluble in tetrahydrofuran (THF), which brings an environmentally friendly device fabrication for solution‐processed OLEDs instead of most widely used chlorinated solvents when 5CzBP is employed as the bulk‐phase of organic host or non‐doped emitter in the emissive layer. 5CzBP exhibits thermally activated delayed fluorescence (TADF) characteristic with relatively high triplet energy of 2.60 eV and a low ΔEST of 0.01 eV. By using the new TADF material as organic host for another green TADF emitter, maximum external quantum efficiency (EQE) of 12.5% has been achieved in simple solution‐processed OLED device. Besides, a maximum EQE of 8.9% and 5.7% was further obtained in TADF devices based on 5CzBP as dopant and non‐doped emitter, respectively. The simultaneously acting as efficient TADF host and non‐doped TADF emitter provides the potential guidance of the future simple single‐layer two‐color white OLEDs based on low‐cost pure organic TADF materials.  相似文献   
7.
本文通过多步有机反应制备了化合物9-苯基-9′-(4-二苯基氧化膦)苯基-氧杂蒽[diphenyl(4-(9-phenyl-9H-xanthen-9-yl)phenyl)phosphine oxide,DPPO],低温磷光发射光谱测试表明该化合物具有高的三线态能级(2.88eV),它可以作为天蓝色磷光发光材料双(4,6-二氟苯基吡啶-N,C2)吡啶甲酰合铱[bis(3,5-difluoro-2-(2-pyridyl)phenyl-(2-carboxypyridyl)iridium(Ⅲ),FIrpic,ET=2.62eV]的主体材料.将主体材料DPPO用于蓝色磷光有机发光二极管中,该器件在100cd/m2的亮度下,电流效率和流明效率分别达到30.6cd/A和19.2lm/W,最大外量子效率达到13.6%.  相似文献   
8.
采用微波辐射加热方法,将2,3-二苯基喹喔啉(DPQ)与水合三氯化铱(IrCl3•H2O)反应,合成了一种新型三环喹喔啉铱配合物[Ir(DPQ)3],通过元素分析,1H NMR和质谱方法对配合物结构进行了表征,并初步研究了配合物的吸收光谱和荧光光谱。结果表明,配合物Ir(DPQ)3在387和458nm处存在单线态1MLCT(金属到配体的电荷跃迁)和三线态3MLCT的吸收;在634nm 处有较强的金属配合物三线态的磷光发射。  相似文献   
9.
有机电致发光器件因在全彩平板显示和固态照明领域中具有广阔的应用前景, 而受到人们的广泛关注。 时至今日, 与现有的红色和绿色有机电致发光材料和器件相比, 具有优越综合性能的蓝色有机电致发光材料和器件却始终匮乏。 相对而言, 蓝光材料具有较宽的能隙, 因而很难获得低电压、高效率和良好稳定性的深蓝光器件。 通常, 白色有机电致发光器件可以通过混合三基色或者两种颜色的方法获得。 但是无论哪种方法, 蓝光材料均是必不可少的。 另外, 还可以通过能量传递将蓝光转化为红光和绿光。 因此, 研发出具有优越综合性能的蓝光材料对有机电致发光器件的推广及应用十分关键。 本文综述了近年来蓝色荧光材料、蓝色磷光材料的研究进展以及蓝光材料在蓝色和白色有机电致发光器件中的应用, 并结合现有工作, 对蓝色有机电致发光材料的研究和应用前景进行展望。  相似文献   
10.
The success of organic light emitting diodes (OLED) has been witnessed by the commercialization of this technology for manufacturing the vivid and colorful displays used in our daily life now. The prospective growth of OLED technology on display industry will be optimistic. Over the last three decades, many different approaches on material and device designs have been implemented for improving the efficiency and stability of OLED devices. These efforts install main cornerstones to support the great achievement of OLED technology. However, until now, the performance and stability of blue OLEDs still have some concerns. This troublesome issue should be totally conquered before the large‐scale manufactures dominated over other display technologies, particularly liquid crystal‐based displays, takes place. Though significant progress has already been made to achieve high performance and long lifetime blue OLEDs, this topic still remains as one of the hot researches in OLEDs. We have been working on this area for about two decades and made some notable contributions. Consequently, in this personal account we have outlined our efforts to obtain better performing blue OLEDs by utilizing a range of emitters based on fluorescence, phosphorescence, delayed fluorescence and exciplex systems. We have also developed some novel host materials for blue OLEDs, which are worth mentioning in this account.  相似文献   
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